The influence of supercritical carbon dioxide parameters on cellulose acetylization and properties of cellulose acetates

The possibility of cellulose diacetate production by direct acetylation of sulfite pulp with acetic anhydride in supercritical carbon dioxide (SC CO₂) is demonstrated. Optimum acetic anhydride to cellulose ratio and parameters of SC CO₂ are selected.     

Raman spegtroscopy of the structure of polysagcharide acetates

Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 54, No. 1, pp. 108–112, January, 1991.     

切伦柯夫相互作用中分段式慢波结构与均匀慢波结构的比较研究

 分析了切伦柯夫束波相互作用中使用单段慢波结构的缺点。指出在分段式慢波结构中，漂移段及其两端的慢波结构组成一Bragg谐振腔，当漂移段长度合适时，根据渡越时间效应理论，这种结构能减小调制束中电子的速度分散，提高束波转化效率。通过粒子模拟方法，比较了均匀慢波结构与分段式慢波结构中束波相互作用的物理图像，验证了理论分析结果，并说明了后者有束密度群聚充分，束电子速度分散小，产生微波功率高、频谱质量好，最佳工作电流大，输入电功率高等优点。     

切伦柯夫相互作用中分段式慢波结构与均匀慢波结构的比较研究

分析了切伦柯夫束波相互作用中使用单段慢波结构的缺点。指出在分段式慢波结构中,漂移段及其两端的慢波结构组成一Bragg谐振腔,当漂移段长度合适时,根据渡越时间效应理论,这种结构能减小调制束中电子的速度分散,提高束波转化效率。通过粒子模拟方法,比较了均匀慢波结构与分段式慢波结构中束波相互作用的物理图像,验证了理论分析结果,并说明了后者有束密度群聚充分,束电子速度分散小,产生微波功率高、频谱质量好,最佳工作电流大,输入电功率高等优点。     

Domain structure of cellulose triacetate

The topology of the surface of thin films obtained from cellulose triacetate solutions has been studied using electron microscopy. The domain structure of the physical network of macromolecules (percolation cluster) with the maximum size L ≈ 30 nm of regions with a local orientational order has been established. With an increase in the volume fraction Ω of the cluster to the critical value Ω = 0.91, repacking of domains takes place, which is connected with a decrease in the parameter Ω, L doubling bifurcation of the size L, and formation of regions of long-range orientational order: the mesophase of the polymer.     

Modeling cochlear dynamics: interrelation between cochlea mechanics and psychoacoustics

A model of the cochlea was used to bridge the gap between model approaches commonly used to investigate phenomena related to otoacoustic emissions and more filter-based model approaches often used in psychoacoustics. In the present study, a nonlinear and active one-dimensional transmission line model was developed that accounts for several aspects of physiological data with a single fixed parameter set. The model shows plausible excitation patterns and an input-output function similar to the linear-compressive-linear function as hypothesized in psychoacoustics. The model shows realistic results in a two-tone suppression paradigm and a plausible growth function of the 2f(1)-f(2) component of distortion product otoacoustic emissions. Finestructure was found in simulated stimulus-frequency otoacoustic emissions (SFOAE) with realistic levels and rapid phase rotation. A plausible "threshold in quiet" including finestructure and spontaneous otoacoustic emissions (SOAE) could be simulated. It is further shown that psychoacoustical data of modulation detection near threshold can be explained by the mechanical dynamics of the modeled healthy cochlea. It is discussed that such a model can be used to investigate the representation of acoustic signals in healthy and impaired cochleae at this early stage of the auditory pathway for both, physiological as well as psychoacoustical paradigms.     

The investigation of the interaction between oxybutynin hydrochloride and bovine serum albumin by spectroscopic methods

The mutual interaction of oxybutynin hydrochloride (OB) with bovine serum albumin (BSA) was investigated by fluorescence, UV–vis absorption, circular dichroism (CD), and Fourier transform infrared (FT-IR) spectroscopies under simulative physiological conditions. The results of fluorescence titration revealed that OB could quench the intrinsic fluorescence of BSA by static quenching and there was a single class of binding sites on BSA for this drug. The thermodynamic parameters ΔH, ΔS, and ΔG calculated at different temperatures indicated that hydrogen bonds and van der Waals interactions were the dominant intermolecular forces in stabilizing the OB–BSA complexes. According to the theory of Förster’s non-radiation energy transfer, the binding distance r between OB and BSA was evaluated to be 3.27 nm. The displacement experiments confirmed that OB could bind to site I of BSA. The FT-IR and CD spectra showed that the binding of OB to BSA induced conformational changes in BSA.